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- source_evidence_literature type ECO_0000212 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- befree-2016 importedOn "2016-02-19" NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion wasGeneratedBy ECO_0000203 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion wasDerivedFrom befree-2016 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion SIO_000772 17914928 NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion evidence source_evidence_literature NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.